Cell recognition and the immune system Flashcards

1
Q

How does body recognise cells

A

Specific molecules, mostly proteins, on cell-surface that are highly specific to pathogens, other cells, toxins and abnormal body cells, and normal body cells.

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2
Q

How body recognises body cells

A

When fetus, lymphocytes constantly colliding with other cells (exclusively with own cells).
Lymphocytes with receptors for own cells are suppressed and die.
Lymphocytes produced in bone marrow that respond to self antigens undergo apoptosis before maturing.

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3
Q

Phagocytosis

A

Chemical products of toxins and dead, damaged, abnormal cells attract phagocytes which attach to the chemicals on surface of pathogen using receptors.
Engulf pathogen to form vesicle known as phagosome.
Lysozymes then hydrolyse the bacteria and products are absorbed into cytoplasm.

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4
Q

Antigen

A

Part of organism that is recognised as non-self by immune system and stimulates response.
Usually proteins on plasma membranes of cells.

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5
Q

How can T-cells differentiate invader cells from normal

A

Phagocytes can display a hydrolysed pathogen’s antigens on surface membrane OR body cells invaded by virus can display virus antigens on surface OR transplanted cells have foreign antigens OR cancer cells present different antigens.

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6
Q

Cell-mediated immunity

A
  • Pathogens invade and phagocyte places antigens from pathogen on cell-surface membrane.
  • Receptors from helper T cell fit exactly to antigens and activates T cell to divide rapidly by mitosis.
  • Cloned T cells develop into memory cells to enable rapid response in future, stimulate phagocytes, stimulate B cells to divide and secrete antibodies, activate cytotoxic T cells.
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7
Q

How do cytotoxic T cells kill

A

Produce protein called perforin that makes holes in cell-surface membrane to make it freely permeable, works well against viruses because sacrifice of body cells.

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8
Q

Humoral immunity

A
  • Surface antigens of invading pathogen bind to complementary surface antibody on B cell and taken in by endocytosis and presented on surface.
  • Activated helper T cells attach to processed antigens and activate the B cell.
  • B cell then divides by mitosis to produce plasma cells and memory cells.
  • Plasma cells secrete many antibodies but survive a few days and memory cells are responsible for secondary response.
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9
Q

What is secondary response

A

Future infections responded to by memory cells dividing rapidly into plasma cells that secrete antibodies to kill cell.

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10
Q

Antibody def

A

Proteins with binding complexes synthesised by B cells, complementary to a specific antigen.

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11
Q

Structure of an antibody

A

4 polypeptide chains. Two heavy chains and 2 light chains. Binding site is different on each and called the variable region that consists of sequence of amino acids to form 3D shape. Binds to form antigen-antibody complex.
Rest of antibody known as constant region. Constant region binds to receptors on B cells.
Hinge region allows flexibility to bind to more than one antigen

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12
Q

How does antibody help kill a pathogen

A

They can clump bacterial cells together (agglutination) to make them easier to locate by phagocytes as less spread out.
Can act as markers to stimulate phagocytes to engulf pathogen.

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13
Q

Targeting medication to cancer cells by attaching a therapeutic drug to an antibody

A

Monoclonal antibodies have receptors specific to cancer cells.
They attach themselves to cancer cells and block uncontrolled growth or kill cancer cells using radiation.
No side effects.

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14
Q

Monoclonal antibodies in medical diagnosis

A

Using monoclonal antibody that interacts with protein produced as a symptom of a disease means that the level of the protein as a symptom can be measured.

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15
Q

Monoclonal antibodies in pregnancy tests

A

Placenta produces a hormone hCG that can be found in urine.
Monoclonal antibodies are linked to coloured particles and binds to hCG if present. Antigen-antibody substrate complex moves across strip until stopped by different type of antibody to make coloured line.

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16
Q

Ethics of monoclonal antibodies

A

Mice are used to produce antibodies by deliberately giving them cancer.
Deaths associated with the use of MA in multiple sclerosis. Patients must have full knowledge of risks and benefits (informed consent).
Testing for safety of MA presents dangers.

17
Q

Passive immunity

A

Produced by introduction of antibodies from an outside source. No direct contact with pathogen and antibodies produced externally. E.g. antivenom given to snake bite victims and baby gaining immunity from mother across placenta.

18
Q

Natural active immunity

A

Individual infected with disease and body produces own antibodies.

19
Q

Artificial active immunity

A

Inducing immune response without suffering symptoms

20
Q

Features of successful vaccine/vaccination programme

A

Economically viable.
Few side effects.
Transportation and storage easy
Possible to vaccinate enough individuals for herd immunity.

21
Q

What is herd immunity?

A

Sufficiently large proportion of population vaccinated to make it difficult for pathogen to spread. Protects individuals who are not vaccinated.

22
Q

Why is herd immunity important?

A

Not possible to vaccinate every single member of population as they are too young or have compromised immune systems.

23
Q

How might vaccination not eliminate a disease?

A

Fails to induce immunity in defective immune systems.
Individuals not vaccinated early enough.
Pathogen can mutate so antigens change (antigenic variability).
Too many varieties of pathogen.
Pathogens conceal in cells or intestines.
Unfounded reasoning for rejections.

24
Q

Ethics of using vaccine

A

Uses animals to produce vaccines.
Side effects that may cause long term harm.
Individuals tested at risk.
Whether it should be compulsory and what terms can be opted out on.
Expenses when diseases are almost wiped.

25
Q

Structure of HIV

A

Lipid envelope with attachment proteins embedded.

Inside is capsid that encloses two strands of RNA and enzymes, including reverse transcriptase to convert DNA from RNA.

26
Q

How does HIV replicate

A
  • Proteins on HIV bind to CD4 protein on T helper cells and fuses with cell surface membrane to inject RNA and reverse transcriptase.
  • Reverse transcriptase converts virus’ RNA to DNA and inserted into cell’s nucleus.
  • HIV DNA in cell means mRNA is created that contains instructions for making new viral protein.
  • New HIV particles made by protein synthesis and HIV particles take part of cell surface membrane for lipid envelope.
27
Q

How does HIV cause AIDS

A

HIV interferes with the functioning of T helper cells.
T helper cells important for cell mediated immunity and humoral immunity therefore no antibodies or memory cells.
Opportunistic infections occur due to weak immune system.

28
Q

ELISA test

A

Enzyme linked immunosorbent assay
Uses antibodies to detect presence of protein and also quantity.
Apply antigen to slide and wash.
Apply specific antibody and wash.
Apply secondary antibody that has enzyme attached.
Add colourless substrate for enzyme and enzyme acts to create coloured product.
Amount of antigen proportional to intensity of colour.

29
Q

Why are antibiotics ineffective against viral diseases

A

Viruses are not alive. They are particles and not cells and do not have metabolisms or cell structure to disrupt.

30
Q

What is monoclonal antibody

A

Antibodies that have the exact same tertiary structure.